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1.
Euro Surveill ; 16(13)2011 Mar 31.
Article in English | MEDLINE | ID: mdl-21489374

ABSTRACT

Plasmodium falciparum malaria is endemic in Haiti, but epidemiological data are scarce. A total of 61 cases of malaria were diagnosed between November 2010 and February 2011 among 130 Haitian patients with undifferentiated fever. Three additional cases were diagnosed in expatriates not taking the recommended chemoprophylaxis. No cases were diagnosed among aid workers using chemoprophylaxis. In conclusion, malaria is a significant health problem in Leogane, Haiti. Aid workers and visitors should use chemoprophylaxis according to existing guidelines.


Subject(s)
Malaria, Falciparum/epidemiology , Adolescent , Adult , Aged , Antimalarials/therapeutic use , Child , Child, Preschool , Chloroquine/therapeutic use , Earthquakes , Female , Haiti/epidemiology , Humans , Malaria, Falciparum/prevention & control , Male , Middle Aged , Observation , Primary Health Care , Prospective Studies , Relief Work , Young Adult
2.
Am J Med Genet ; 35(1): 85-90, 1990 Jan.
Article in English | MEDLINE | ID: mdl-2301474

ABSTRACT

The clinical manifestations of various degrees of mental retardation, spastic diplegia, and deaf mutism are known as the neurologic type of endemic cretinism (EC), occurring in countries with high goiter endemicity. Maternal iodine deficiency has been established as the major cause in EC, whereas a genetic predisposition has not been well-documented. Genetic data on 70 families with EC from Highland Ecuador are reported. A segregation analysis of 49 fully classified families yielded an estimate of P = 0.245 (var [P] = 0.00167). Half-sibs were all unaffected and no significant birth order effect was observed among 101 probands. The data indicate an autosomal recessive predisposition as a major etiological factor. Because the neurologic type of EC represents a defined section of the spectrum of iodine deficiency disorders (IDD), the term fetal iodine deficiency disorder (FIDD) rather than cretinism is suggested. The clinical findings in 70 patients were used to delineate the minimal diagnostic criteria of FIDD.


Subject(s)
Congenital Hypothyroidism/genetics , Deafness/genetics , Fetal Diseases/etiology , Iodine/deficiency , Abnormalities, Multiple/etiology , Anthropometry , Congenital Hypothyroidism/metabolism , Dermatoglyphics , Ecuador , Female , Genes, Recessive , Humans , Male , Pedigree , Pregnancy
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